Manufacturing Associate - Cell Therapy

SOKOL GxP Services; Bothell (WA); On-site; USD 29,000 - 33,000; Full time

Benefits offered by this job

Health insurance with dental andVision

Holiday pay

401(k) program

Employee referral bonus program

Job summary

SOKOL GxP Services in Bothell, WA is seeking an entry-level Manufacturing Associate to support cell therapy production in a regulated biopharmaceutical environment. The role involves hands-on manufacturing, equipment preparation, GMP documentation, and cleanroom teamwork.

You will follow SOPs, weigh materials, sanitize equipment, monitor processes, maintain aseptic conditions, and complete production records. This 12-month onsite position offers growth, rotating schedule, and a W-2 arrangement.

Qualifications

• High school diploma or equivalent.
• Associate or Bachelor's degree in life sciences preferred.
• 0–2 years of cGMP manufacturing experience preferred.
• Experience with SOPs, cleanroom operations and aseptic processing.
• Authorization to work in the United States without visa sponsorship.

Responsibilities

• Perform routine manufacturing operations following approved SOPs and work instructions.
• Weigh and verify raw materials, assemble and sanitize production equipment, and monitor manufacturing processes.
• Maintain cleanroom conditions and follow cGMP and aseptic processing requirements.
• Complete production documentation and identify or escalate process deviations.
• Learn manufacturing systems, including electronic work instructions and production records.
• Support inventory management, process documentation, and safe manufacturing practices.
• Collaborate with manufacturing teams to maintain production quality and efficiency.

Skills

Communication

Teamwork

Documentation

Computer literacy

Attention to detail

Education

High school diploma

Life sciences degree (Assoc/Bachelor)

Tools

Syncade MES

Oracle

Job description

We are seeking a Manufacturing Associate to support cell therapy production in a regulated biopharmaceutical manufacturing environment. This entry-level opportunity involves hands‑on production activities, equipment preparation, GMP documentation, and teamwork in a cleanroom setting.

Key responsibilities:

• Perform routine manufacturing operations following approved SOPs and work instructions;
• Weigh and verify raw materials, assemble and sanitize production equipment, and monitor manufacturing processes;
• Maintain cleanroom conditions and follow cGMP and aseptic processing requirements;
• Complete production documentation and identify or escalation process deviations;
• Learn manufacturing systems, including electronic work instructions and production records;
• Support inventory management, process documentation, and safe manufacturing practices;
• Collaborate with manufacturing teams to maintain production quality and efficiency.

Position details:

• Hourly rate: $21.14–$24.14;
• Contract length: 12 months with possible extension;
• Location: Bothell, WA;
• Work arrangement: 100% onsite;
• Schedule: Sunday–alternate Wednesday, 11:00 AM–11:30 PM, rotating schedule;
• W-2 contract position;
• No C2C options;
• No visa sponsorship.

Required:

• High school diploma or equivalent combination of education and experience;
• Ability to follow written manufacturing procedures and maintain accurate documentation;
• Strong attention to detail and ability to identify and elevate deviations;
• Good communication, interpersonal, and teamwork skills;
• Proficiency with basic computer applications;
• Ability to work onsite on the assigned rotating shift;
• Ability to work in a cleanroom environment using required gowning and PPE;
• Ability to stand or walk for extended periods, lift up to 30 pounds, and push or pull up to 50 pounds;
• Authorization to work in the United States without visa sponsorship.

Preferred:

• Associate’s or Bachelor’s degree in life sciences;
• 0–2 years of cGMP manufacturing experience or equivalent relevant education or experience;
• Experience with SOPs, cleanroom operations, and aseptic processing;
• Experience in regulated environments, including regulatory inspections;
• Familiarity with Syncade MES, Oracle, ETQ, BMRAM, or similar systems;
• Experience with electronic manufacturing documentation, equipment management, or inventory management systems.

• Health insurance with dental and vision insurance options.
• Holiday pay.
• 401(k) program.
• Employee referral bonus program.
• The client retains the right to hire the contractor directly.